Canonical Allele Identifier: PA2825541719
Gene: ADAR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Pro3Ala
CA342612244
NM_001111.5:c.7C>G